{{Rsnum
|rsid=58599399
|Gene=PRPH
|Chromosome=12
|position=49295621
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=PRPH,RP11-161H23.9
}}{{omim
|id=170710
|rsnum=58599399
|variant=0002
}}

{{ClinVar
|rsid=58599399
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=49689404
|CHROM=12
|GMAF=0.0014
|dbSNPBuildID=135
|SSR=0
|SAO=1
|VP=0x050160000000000016110100
|GENEINFO=PRPH:5630
|GENE_NAME=PRPH
|GENE_ID=5630
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.49689404G>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNACC=RCV000014706.1; RCV000057167.1
|CLNDBN=Amyotrophic lateral sclerosis, susceptibility to; not provided
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNSRCID=PRPH:c.421G>T; 170710.0002
|COMMON=0
|Disease=Amyotrophic lateral sclerosis; not provided
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}